ccdc reference numbers (Cambridge Crystallographic)
86
Structured Review
Cambridge Crystallographic
ccdc reference numbers
Ccdc Reference Numbers, supplied by Cambridge Crystallographic, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/reference+numbers/ccdc+numbers/pm42234756-201-2-19
Average 86 stars, based on 1 article reviews
Ccdc Reference Numbers, supplied by Cambridge Crystallographic, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/reference+numbers/ccdc+numbers/pm42234756-201-2-19
Average 86 stars, based on 1 article reviews
ccdc reference numbers - by Bioz Stars,
2026-10
86/100 stars
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other:Article Title: Stable zero-dimensional hybrid indium-based halides with yellow to orange light emission. Article Snippet: Low-dimensional organic–inorganic hybrid materials (OIHMs) in the field of luminescence have been occupying promising application prospects, but the toxicity and instability of lead-based halides are huge obstacles to the industrial utilization of these materials.. Developing lead-free halides with low-toxicity and high stability have become important topics of research in recent years.. Herein, we report three 0D Inbased OIHMs (ABI)3(InBr6)Br (ABI = 2-aminium benzo-imidazole) 1, (DMA)4(InBr6)Br (DMA = dimethylammonium) 2, and (BAPP)(InBr6)Br·6H2O (BAPP = 1,4-bis(3-aminopropyl)piperazine) 3, which show maximum emission peaks within 605–622 nm, with a photoluminescence quantum yield (PLQY) of 60.80% being the highest achieved. Article Title: Delocalizing electron distribution in thermally activated delayed fluorophors for high-efficiency and long-lifetime blue electroluminescence. Article Snippet: Blue thermally activated delayed fluorescent emitters are promising for the next generation of organic light-emitting diodes, yet their performance still cannot meet the requirements for commercialization.. Here we establish a design rule for highly efficient and stable thermally activated delayed fluorescent emitters by introducing an auxiliary acceptor that could delocalize electron distributions, enhancing molecular stability in both the negative polaron and triplet excited state, while also accelerating triplet-to-singlet up-conversion and singlet radiative processes simultaneously.. Proof-of-concept thermally activated delayed fluorescent compounds, based on a multi-carbazole-benzonitrile structure, exhibit near-unity photoluminescent quantum yields, short-lived delays and improved photoluminescent and electroluminescent stabilities. |
